Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1427407
rs1427407
6 0.827 0.120 2 60490908 intron variant T/C;G snv 0.710 1.000 3 2011 2019
dbSNP: rs11886868
rs11886868
12 0.752 0.280 2 60493111 intron variant C/T snv 0.65 0.710 1.000 2 2011 2016
dbSNP: rs4671393
rs4671393
11 0.790 0.400 2 60493816 intron variant A/C;G snv 0.710 1.000 2 2011 2016
dbSNP: rs766432
rs766432
6 0.925 0.080 2 60492835 intron variant C/A snv 0.80 0.700 1.000 3 2011 2014
dbSNP: rs10172646
rs10172646
2 1.000 0.080 2 60493622 intron variant G/A snv 0.64 0.700 1.000 1 2011 2011
dbSNP: rs10189857
rs10189857
6 1.000 0.080 2 60486100 intron variant A/G snv 0.42 0.700 1.000 1 2011 2011
dbSNP: rs10195871
rs10195871
2 1.000 0.080 2 60493454 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1896294
rs1896294
2 1.000 0.080 2 60491939 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1896295
rs1896295
2 1.000 0.080 2 60496951 intron variant T/C snv 0.81 0.700 1.000 1 2011 2011
dbSNP: rs1896296
rs1896296
2 1.000 0.080 2 60496952 intron variant G/T snv 0.80 0.700 1.000 1 2011 2011
dbSNP: rs6545816
rs6545816
2 1.000 0.080 2 60487726 intron variant A/C;G snv 0.50 0.700 1.000 1 2011 2011
dbSNP: rs6545817
rs6545817
2 1.000 0.080 2 60488044 intron variant C/T snv 0.49 0.700 1.000 1 2011 2011
dbSNP: rs6706648
rs6706648
2 1.000 0.080 2 60494905 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs6729815
rs6729815
4 1.000 0.080 2 60496537 intron variant T/C snv 0.49 0.700 1.000 1 2011 2011
dbSNP: rs6738440
rs6738440
2 1.000 0.080 2 60495106 intron variant A/G snv 0.26 0.700 1.000 1 2011 2011
dbSNP: rs7557939
rs7557939
2 1.000 0.080 2 60494212 intron variant G/A snv 0.64 0.700 1.000 1 2011 2011
dbSNP: rs7565301
rs7565301
3 1.000 0.080 2 60496131 intron variant G/A snv 0.25 0.700 1.000 1 2011 2011
dbSNP: rs7584113
rs7584113
2 1.000 0.080 2 60494176 intron variant A/G snv 0.64 0.700 1.000 1 2011 2011
dbSNP: rs7599488
rs7599488
4 0.925 0.120 2 60491212 intron variant C/T snv 0.42 0.700 1.000 1 2011 2011
dbSNP: rs7606173
rs7606173
5 1.000 0.080 2 60498316 intron variant G/C;T snv 0.39 0.700 1.000 1 2011 2011